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    Job · 21252543

    VADODARA · FULLTIME

    Assistant Manager - Regulatory Affairs

    Novumgen

    Novumgen

    Vadodara · onsite · Posted 5d ago

    Sourced fromFoundit
    Not disclosed6–8 yrsfulltimeVadodara

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    Section · 01

    About this role

    Regulatory Affairs – Strategy Team

    Post Approvals – UK / EU

    Position: Senior Executive / Assistant Manager

    Experience: 6+ years

    Job Responsibilities:

    • Regulatory expert responsible for the submissions, RFIs and compliance activities commercial products supporting Business Unit.
    • Leads the preparation of CMC information for submission to global regulatory agencies, generates and drives CMC strategies, assesses risks and develops mitigation plans.
    • Provide regulatory direction and documentation for assigned projects/products covering initial registrations and approval/post approval activities, for regional products registered specifically for EU/AU/CA/UK markets.
    • Acts as the SPOC for Strategy Alliance Team - Global regulatory representative within cross-functional teams, involving the interpretation of regulations and guidelines and the assessment of global implications for strategic regulatory decisions.
    • Accountable for interactions with regulatory agencies and external partners either directly or in conjunction with other stake holders.
    • Operate independently to resolve issues and manage regulatory risks and ambiguous situations within project teams.
    • Investigates opportunities for regulatory innovation / promote the use of novel approaches within project team to resolve issues and problems. May take appropriate risk to achieve desired results.

    Details of the job responsibilities to be performed

    1. In-licensing product due diligence and timely circulation of the assessment reports.
    2. UK, EU, US and Canada dossier review and submission.
    3. Provide regulatory support to cross functional teams.
    4. Review of Tech Transfer documents and Product development data.
    5. Review of GMP documents of Contract Manufacturers.
    6. Preparation and review of regulatory strategy documents for newly introduced products.
    7. Communicate with different regulatory agencies and partners for timely information availability.
    8. eCTD development support for different regions.
    9. Timely submission and approval of Marketing authorizations.
    10. Responsible for all business query response

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    Section · 02

    Skills

    eCTD developmentdossier reviewCMC strategies

    Section · Company

    About Novumgen

    Novumgen

    Novumgen

    Pharma

    50

    employees

    2021

    5 years old

    Vadodara, Gujarat

    India

    About

    Novumgen is a global pharmaceutical company developing innovative medicines across oncology, immunology, anti-infectives, and rare diseases.

    Industries

    PharmaBiotechnologyClinical ResearchHealthcare

    Employee ratings

    87 reviews

    4.1/ 5

    Culture

    4.1

    Career growth

    3.7

    Work-life

    4.0

    Employees rate it well for

    Learning21Career Growth15Senior Management13Work Environment8Work Culture6

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